Castleman病:沙特阿拉伯儿科意外病例1例报告。

IF 0.5 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-09-13 eCollection Date: 2025-09-01 DOI:10.1093/jscr/rjaf712
Hussain A Alessa, Afnan N Alshayeb, Tahani M Alqurashi, Munira A Suwailem, Ali M Alghamdi, Fahad F Elmokyed, Tahar Yacoubi
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引用次数: 0

摘要

Castleman病是一种罕见的淋巴细胞增生性疾病,病因不明,其最常见的症状是纵隔淋巴结肿物。虽然它在年轻人中很少见,但在成年人中很普遍。我们报告一个病例14岁的男孩谁是入院的外科急性右侧腹痛,怀疑急性阑尾炎。术前腹部影像学检查显示炎性阑尾及大肠系膜肿块。经组织病理学检查证实为急性阑尾炎及单中心肠系膜肿块,经腹腔镜手术切除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Castleman disease: a case report of a pediatric incidental case in Saudi Arabia.

Castleman disease: a case report of a pediatric incidental case in Saudi Arabia.

Castleman disease: a case report of a pediatric incidental case in Saudi Arabia.

Castleman disease: a case report of a pediatric incidental case in Saudi Arabia.

The most prevalent symptom of Castleman disease, a rare lymphoproliferative condition with an unclear etiology, is a mediastinal nodal mass. While it is quite uncommon in youngsters, it is prevalent in adults. We report a case of a 14-year-old boy who was admitted to the department of surgery for acute right-sided abdominal pain, with suspected acute appendicitis. Preoperative imaging investigation of the abdomen showed an inflammatory appendix as well a large mesenteric mass. Histopathology examination confirmed the diagnosis of acute appendicitis and mesenteric mass unicentric Castleman after resection by laparoscopic approach.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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